Taiwan FDA registration 101d633dab51a4bcbb3ea66d1f462e68

"Pierre Rolland" Fiber Post (Non-Sterile)

TW: "碧籃" 玻璃纖維牙根柱 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·OVERFIBERS S.R.L.·Registered Mar 26, 2018 – Mar 26, 2028Active
Registration details
Analysis ID
101d633dab51a4bcbb3ea66d1f462e68
License Form
Ministry of Health Medical Device Import No. 018926
Customs Code
DHA09401892608
Company information
Manufacturer
OVERFIBERS S.R.L.
Manufacturer Country
Italy
Authorized Representative
LA FU INDUSTRIAL CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Center Column Nail (F.3810)".
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F3810 tube center column nail
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 26, 2018
Expiry Date
Mar 26, 2028
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About this record

Access comprehensive regulatory information for "Pierre Rolland" Fiber Post (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 101d633dab51a4bcbb3ea66d1f462e68 and manufactured by OVERFIBERS S.R.L.. The authorized representative in Taiwan is LA FU INDUSTRIAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PRODUITS DENTAIRES PIERRE ROLLAND SAS, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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